Characteristics of the slow inhibitory postsynaptic potential of bullfrog symphathetic ganglion cells

Life Sciences ◽  
1967 ◽  
Vol 6 (17) ◽  
pp. 1827-1836 ◽  
Author(s):  
K. Koketsu ◽  
S. Nishi
1989 ◽  
Vol 61 (6) ◽  
pp. 1110-1120 ◽  
Author(s):  
M. J. Korenberg ◽  
H. M. Sakai ◽  
K. Naka

1. Three independent sets of evidence have been obtained to show that similar first- and second-order light-evoked kernels are computed for the ganglion cell when the system output is taken to be either the spike train (discrete signal) or the postsynaptic potential (analog signal). In this paper we show that the similarity of postsynaptic potential (PSP) kernels and spike kernels is readily explained by assuming an underlying cascade structure for the neural information processing. The cascade structure enables spike kernels to be mathematically related very simply to the process of generating the postsynaptic potentials of ganglion cells. 2. Mathematical analysis of the cascade structure also suggests why spike kernels appear to differ slightly from PSP kernels. The relation between the two sets of kernels predicted from our analysis is substantiated here by experiment and reveals an interconnection between several of the signals measured. 3. Our experimental results, in particular, suggest that the neuronal circuitry leading from the light stimulus to the generation of ganglion cell spike discharges can be represented as follows: either a Wiener (LN) or a dynamic linear-static nonlinear-dynamic linear (LNL) structure is followed by a highly nonlinear process [static or brief-memory Hammerstein static-nonlinear dynamic-linear (NL) structure] of spike generation. Cross-correlation between the analog input and spike output enables identification of these structures.


1988 ◽  
Vol 66 (8) ◽  
pp. 1100-1102 ◽  
Author(s):  
Paul Perreault ◽  
Massimo Avoli

We report that CA1 pyramidal neurons of the rat hippocampus respond to high intensity afferent stimulation by generating a late depolarizing potential that typically occurs between the early (fast) inhibitory postsynaptic potential (IPSP) and the late (slow) IPSP. This potential is reminiscent of the response seen after the application of 4-aminopyridine and can be blocked by bicuculline, indicating that GABAA receptors are involved in its generation.


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